Variant report

Variant	rs62367844
Chromosome Location	chr5:57886077-57886078
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11955748	1.00[ASN][1000 genomes]
rs12152846	1.00[ASN][1000 genomes]
rs1422230	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17712820	1.00[ASN][1000 genomes]
rs35454977	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60365444	1.00[ASN][1000 genomes]
rs60630307	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62367812	0.97[ASN][1000 genomes]
rs62367813	1.00[ASN][1000 genomes]
rs62367814	0.99[ASN][1000 genomes]
rs62367815	1.00[ASN][1000 genomes]
rs62367816	0.99[ASN][1000 genomes]
rs62367842	1.00[ASN][1000 genomes]
rs6896790	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7723416	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57886000-57889600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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